{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,5,4]],"date-time":"2026-05-04T21:14:02Z","timestamp":1777929242904,"version":"3.51.4"},"reference-count":51,"publisher":"SAGE Publications","issue":"3","license":[{"start":{"date-parts":[[2026,1,5]],"date-time":"2026-01-05T00:00:00Z","timestamp":1767571200000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/journals.sagepub.com\/page\/policies\/text-and-data-mining-license"}],"content-domain":{"domain":["journals.sagepub.com"],"crossmark-restriction":true},"short-container-title":["Lupus"],"published-print":{"date-parts":[[2026,3]]},"abstract":"<jats:sec>\n                    <jats:title>Background<\/jats:title>\n                    <jats:p>Recently, Cytotoxic T lymphocyte-associated antigen-4 (CTLA-4) gene has emerged as an attractive candidate gene implicated in susceptibility to autoimmune disease such as Juvenile-onset SLE (JSLE).<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Objective<\/jats:title>\n                    <jats:p>\n                      To investigate\n                      <jats:italic toggle=\"yes\">CTLA-4<\/jats:italic>\n                      exon 1 + 49A\/G (rs231775)\n                      <jats:italic toggle=\"yes\">SNP<\/jats:italic>\n                      as a genetic marker for susceptibility to JSLE and lupus nephritis in Egyptian children and adolescents.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>\n                      This prospective case-control study included 260 patients diagnosed with Juvenile-onset SLE, and 260 healthy controls. We genotyped all participants for CTLA-4 (A\/G) (rs231775)\n                      <jats:italic toggle=\"yes\">SNP<\/jats:italic>\n                      located in exon 1 at position 49 by polymerase chain reaction.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      The\n                      <jats:italic toggle=\"yes\">CTLA-4<\/jats:italic>\n                      exon 1 + 49\n                      <jats:italic toggle=\"yes\">G\/G<\/jats:italic>\n                      gene variant and\n                      <jats:italic toggle=\"yes\">G<\/jats:italic>\n                      allele were significantly more represented in JSLE patients than healthy controls (27% vs 8%; ORs = 4.2; [95% CI: 2.4 \u2013 7.3]; for the\n                      <jats:italic toggle=\"yes\">G\/G<\/jats:italic>\n                      genotype) and (47.5% vs 35%; ORs: 1.7; [95% CIs: 1.3 \u2013 2.2]\n                      <jats:italic toggle=\"yes\">;<\/jats:italic>\n                      for\n                      <jats:italic toggle=\"yes\">G<\/jats:italic>\n                      allele);\n                      <jats:italic toggle=\"yes\">P<\/jats:italic>\n                      &lt; .01. The\n                      <jats:italic toggle=\"yes\">CTLA-4\u00a0G\/G<\/jats:italic>\n                      genotype and\n                      <jats:italic toggle=\"yes\">G<\/jats:italic>\n                      allele were identified as possible risk factors for development of lupus nephritis (for\n                      <jats:italic toggle=\"yes\">G\/G<\/jats:italic>\n                      genotype; ORs: 5.09; [95% CIs: 1.7 - 13.9];\n                      <jats:italic toggle=\"yes\">P<\/jats:italic>\n                      = .0001, and for\n                      <jats:italic toggle=\"yes\">G-<\/jats:italic>\n                      allele; ORs: 2.4; [95% CIs: 1.5 - 3.78];\n                      <jats:italic toggle=\"yes\">P<\/jats:italic>\n                      = .004).\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusion<\/jats:title>\n                    <jats:p>\n                      The\n                      <jats:italic toggle=\"yes\">CTLA-4<\/jats:italic>\n                      exon 1 + 49\n                      <jats:italic toggle=\"yes\">A\/G<\/jats:italic>\n                      polymorphism may confer susceptibility to Juvenile-onset SLE. Moreover,\n                      <jats:italic toggle=\"yes\">CTLA-4\u00a0G\/G<\/jats:italic>\n                      genotype and\n                      <jats:italic toggle=\"yes\">G<\/jats:italic>\n                      allele at exon 1 + 49 may constitute independent risk factors for development of lupus nephritis in Egyptian children and adolescents.\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.1177\/09612033251414929","type":"journal-article","created":{"date-parts":[[2026,1,5]],"date-time":"2026-01-05T18:06:46Z","timestamp":1767636406000},"page":"280-288","update-policy":"https:\/\/doi.org\/10.1177\/sage-journals-update-policy","source":"Crossref","is-referenced-by-count":0,"title":["Association of CTLA-4 exon 1(+49 A\/G) polymorphism and susceptibility to SLE in Egyptian children and adolescents"],"prefix":"10.1177","volume":"35","author":[{"given":"Faika","family":"Arab","sequence":"first","affiliation":[{"name":"Department of Pediatrics, Faculty of Medicine, Zagazig University, Zagazig, Egypt"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Sarah A.","family":"Saleh","sequence":"additional","affiliation":[{"name":"Department of Pediatrics, Faculty of Medicine, Cairo University, Cairo, Egypt"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Dina M.","family":"Ibrahim","sequence":"additional","affiliation":[{"name":"Department of Pediatrics, Faculty of Medicine, Cairo University, Cairo, Egypt"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Amany N.","family":"Barakat","sequence":"additional","affiliation":[{"name":"Department of Pediatrics, Faculty of Medicine, Tanta University, Tanta, Egypt"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Aly A.","family":"Yousef","sequence":"additional","affiliation":[{"name":"Department of Pediatrics, Faculty of Medicine, Capital University (formerly Helwan University), Administrative Capital, Egypt"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Mohamed","family":"Abdulhay","sequence":"additional","affiliation":[{"name":"Department of Pediatrics, Faculty of Medicine, Capital University (formerly Helwan University), Administrative Capital, Egypt"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Mohammed K.","family":"Haridi","sequence":"additional","affiliation":[{"name":"Department of Pediatrics, Faculty of Medicine, Assiut University, Assiut, Egypt"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Marwa M.","family":"Al-Fahham","sequence":"additional","affiliation":[{"name":"Department of Pediatrics, Faculty of Medicine, Ain-Shams University, Cairo, Egypt"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Dalia M","family":"Selim","sequence":"additional","affiliation":[{"name":"Al-Adan New Women &amp; 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